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rs794728598

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728598(G;T)
Make rs794728598(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156114921
GeneLMNA
is asnp
is mentioned by
dbSNPrs794728598
ebirs794728598
HLIrs794728598
Exacrs794728598
Varsomers794728598
Maprs794728598
PheGenIrs794728598
hapmaprs794728598
1000 genomesrs794728598
hgdprs794728598
ensemblrs794728598
gopubmedrs794728598
geneviewrs794728598
scholarrs794728598
googlers794728598
pharmgkbrs794728598
gwascentralrs794728598
openSNPrs794728598
23andMers794728598
23andMe allrs794728598
SNP Nexus

SNPshotrs794728598
SNPdbers794728598
MSV3drs794728598
GWAS Ctlgrs794728598
Max Magnitude0
ClinVar
Risk rs794728598(C,T;C,T)
Alt rs794728598(C,T;C,T)
Reference rs794728598(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156084712G>C; NC_000001.10:g.156084712G>T
CLNSRC
CLNACC RCV000236357.1, RCV000182378.2,